DBA is hard but it’s my child’s life. I have to teach him how to live life with it. I will advocate and help find a cure. The DBAF is helping us improve his life.
Lily loves everyday she has, especially the ones she’s not in the hospital. Lily is the strongest little girl I know, my hero.
Some days are good, others not so good. Please help find a cure for our family.
I am and always will be special. I am and always will be DBA Strong!
We hope for an easier life, until then we are grateful for each day together.
Of all the people on earth, the Lord your God has chosen you to be his own special treasure. -Deuteronomy 7:6
It has been seven years since DBA became part of our vocabulary. Our son’s diagnosis brought confusion, apprehension and despair. The discovery of DBAF is a stroke of serendipity. While even more tears were shed, these are now mingled with knowledge, understanding and, more significantly, hope. It will be through research that our son will be able to secure a brighter future.
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